Postoperative Pain Management in Rhinoplasty: A Double Blind Randomized Controlled Trial
| dc.contributor.author | Kandathil, Cherian Kurian | |
| dc.contributor.author | Spataro, Emily A. | |
| dc.contributor.author | Saltychev, Mikhail | |
| dc.contributor.author | Kalebjian, Roushig | |
| dc.contributor.author | Patel, Priyesh N. | |
| dc.contributor.author | Kim, Cherine H. | |
| dc.contributor.author | Akkina, Sarah R. | |
| dc.contributor.author | Kimura, Kyle S. | |
| dc.contributor.author | Rossi-Meyer, Monica | |
| dc.contributor.author | Longino, Elizabeth S. | |
| dc.contributor.author | Truong, Henry | |
| dc.contributor.author | Most, Sam P. | |
| dc.contributor.organization | fi=fysiatria|en=Physical and Rehabilitation Medicine| | |
| dc.contributor.organization | fi=tyks, vsshp|en=tyks, varha| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.17712075286 | |
| dc.converis.publication-id | 516139624 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/516139624 | |
| dc.date.accessioned | 2026-05-04T20:12:17Z | |
| dc.description.abstract | <h3>Background:</h3><p>There is inadequate evidence for the utilization of nonnarcotic pain medications for postoperative pain management following rhinoplasty.</p><h3>Objective:</h3><p>To compare the effectiveness of opioid and non-opioid medications for postoperative pain control in rhinoplasty as measured by a visual analog scale (VAS) on postoperative days 0–5.</p><h3>Methods:</h3><p>In this double-blind randomized controlled clinical trial, adult patients who underwent primary rhinoplasty at a tertiary center were enrolled from August 2019 to October 2024. Patients were randomized to receive either a combination of acetaminophen (325 mg) and hydrocodone (5 mg) or acetaminophen (325 mg) and ibuprofen (200 mg), 1–2 tablets every 4 h for five postoperative days. Tramadol (50 mg) was prescribed for breakthrough pain.</p><h3>Results:</h3><p>A total of 130 patients (65 per group) completed the study. The average age (SD) was 32 (10.7) years. The majority were women (77%), White (68%), and underwent combined functional and aesthetic rhinoplasty (52%). There was no difference detected in mean postoperative pain (VAS) scores recorded on postoperative days 0–5, between treatment groups (<em>p</em> = 0.156). Among side effects, only itchiness was significantly higher (<em>p</em> = 0.001) in the hydrocodone–acetaminophen group.</p><h3>Conclusion:</h3><p>This trial demonstrates a lack of difference between opioid and non-opioid pain medications in postoperative pain control after rhinoplasty.</p> | |
| dc.identifier.eissn | 2689-3622 | |
| dc.identifier.jour-issn | 2689-3614 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/60293 | |
| dc.identifier.url | https://doi.org/10.1177/26893614261429310 | |
| dc.identifier.urn | URN:NBN:fi-fe2026050438227 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Saltychev, Mikhail | |
| dc.okm.affiliatedauthor | Dataimport, tyks, vsshp | |
| dc.okm.discipline | 3126 Surgery, anesthesiology, intensive care, radiology | en_GB |
| dc.okm.discipline | 3126 Kirurgia, anestesiologia, tehohoito, radiologia | fi_FI |
| dc.okm.internationalcopublication | international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher | Mary Ann Liebert | |
| dc.publisher.country | United States | en_GB |
| dc.publisher.country | Yhdysvallat (USA) | fi_FI |
| dc.publisher.country-code | US | |
| dc.relation.articlenumber | 26893614261429310 | |
| dc.relation.doi | 10.1177/26893614261429310 | |
| dc.relation.ispartofjournal | Facial Plastic Surgery & Aesthetic Medicine | |
| dc.title | Postoperative Pain Management in Rhinoplasty: A Double Blind Randomized Controlled Trial | |
| dc.year.issued | 2026 |
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